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Allopurinol - 63629-1675-2 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 63629-1675
Proprietary Name: Allopurinol
Non Proprietary Name: Allopurinol
Active Ingredient(s): 100    mg/1 & nbsp;   Allopurinol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Allopurinol

Product NDC: 63629-1675
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018832
Marketing Category: NDA
Start Marketing Date: 20090406

Package Information of Allopurinol

Package NDC: 63629-1675-2
Package Description: 30 TABLET in 1 BOTTLE (63629-1675-2)

NDC Information of Allopurinol

NDC Code 63629-1675-2
Proprietary Name Allopurinol
Package Description 30 TABLET in 1 BOTTLE (63629-1675-2)
Product NDC 63629-1675
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090406
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name ALLOPURINOL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]

Complete Information of Allopurinol


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